Brainmaster Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Brainmaster Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: qEEG-Pro
2
Total
2
Cleared
0
Denied
Brainmaster Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Bedford, US.
Historical record: 2 cleared submissions from 2016 to 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Brainmaster Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Brainmaster Technologies, Inc.
2 devices